Suppr超能文献

Chiari I畸形中小脑扁桃体缺血向小脑扁桃体囊肿的演变:放射学、手术及组织学证据

Evolution of cerebellar tonsillar ischemia to cerebellar tonsillar cysts in the Chiari I malformation: radiological, surgical, and histological evidence.

作者信息

Tubbs R Shane, Demerdash Amin, Oskouian Rod J, Chern Joshua J, Oakes W Jerry

机构信息

Seattle Science Foundation, Seattle, WA, USA.

Pediatric Neurosurgery, Children's of Alabama, 1600 7th Ave South, Lowder 400, Birmingham, AL, 35233, USA.

出版信息

Childs Nerv Syst. 2016 Apr;32(4):661-5. doi: 10.1007/s00381-015-2960-7. Epub 2015 Nov 16.

Abstract

BACKGROUND

Rare reports in the literature have documented the presence of a cyst at the tip of the cerebellar tonsil in patients with Chiari I malformation. The current study aimed to better elucidate these cysts and identify their etiology via a histological and radiologically analysis.

PATIENTS AND METHODS

We prospectively reviewed all new Chiari I malformation (CM-I) patients who presented to our clinic during a 2-year period. This was a pediatric cohort made up of 340 children aged 3 to 18 years. Specifically, all patients were screened for ischemic or cystic lesions of the herniated cerebellar tonsils on MRI.

RESULTS

Out of 340 patients, 2.9 % were found to have signal changes on MRI consistent with ischemia or cysts in the cerebellar tonsils. Of the 340 patients, 20 % underwent posterior fossa decompression. Of the 67 patients, cerebellar tonsillar ischemia was observed in 10.4 % and cerebellar tonsillar cysts were seen in 6 %. Four of the seven operative patients with cerebellar tonsillar ischemia and concomitant syringomyelia and three of these patients with tonsillar cysts concomitant syringomyelia and cerebellar tonsillar cysts underwent subpial dissection of some cerebellar tonsil to ensure that CSF egress from the fourth ventricle to the cervical subarachnoid space, and this transected tissue was also sent for histological analysis. Three of the four patients found to have intraoperative tonsillar cysts were noted to have tonsillar ischemic changes on preoperative imaging in this same region. For both ischemic and cystic cerebellar tonsils, histologically, the tissue demonstrated loss of Purkinje cells with concomitant Bergmann gliosis. The ischemic and cystic tissues were virtually the same, histologically.

CONCLUSIONS

Based on our findings, cerebellar tonsillar ischemia and cysts in patients with CM-I can often be seen radiologically. Histologically, these ischemic and cystic tissues are the same. Moreover, we document patients where ischemic lesions progressed to cysts, radiologically. Taken together, cerebellar tonsillar ischemia and cysts are on a continuum and represent chronic compression of this herniated part of the cerebellum.

摘要

背景

文献中鲜有报道记录Chiari I型畸形患者小脑扁桃体尖端存在囊肿。本研究旨在通过组织学和放射学分析更好地阐明这些囊肿并确定其病因。

患者与方法

我们前瞻性地回顾了在两年期间到我们诊所就诊的所有新诊断的Chiari I型畸形(CM-I)患者。这是一个由340名3至18岁儿童组成的儿科队列。具体而言,所有患者均接受MRI检查,以筛查疝出的小脑扁桃体的缺血性或囊性病变。

结果

在340例患者中,2.9%被发现MRI信号改变与小脑扁桃体缺血或囊肿一致。在340例患者中,20%接受了后颅窝减压术。在67例接受手术的患者中,10.4%观察到小脑扁桃体缺血,6%观察到小脑扁桃体囊肿。7例手术患者中有4例伴有小脑扁桃体缺血和脊髓空洞症,其中3例伴有扁桃体囊肿、脊髓空洞症和小脑扁桃体囊肿的患者接受了部分小脑扁桃体的软膜下剥离,以确保脑脊液从第四脑室流入颈蛛网膜下腔,并且将切除的组织送去进行组织学分析。在术中发现有扁桃体囊肿的4例患者中,有3例在术前同一区域的影像学检查中发现有扁桃体缺血改变。对于缺血性和囊性小脑扁桃体,组织学上,组织显示浦肯野细胞丢失并伴有伯格曼胶质细胞增生。缺血性和囊性组织在组织学上几乎相同。

结论

根据我们的研究结果,CM-I患者的小脑扁桃体缺血和囊肿在放射学上经常可见。组织学上,这些缺血性和囊性组织是相同的。此外,我们记录了放射学上缺血性病变进展为囊肿的患者。综上所述,小脑扁桃体缺血和囊肿是连续的,代表了小脑疝出部分的慢性压迫。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验